NM_001005242.3(PKP2):c.2176A>T (p.Thr726Ser) AND Arrhythmogenic right ventricular dysplasia 9
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 11, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001957192.6
Allele description [Variation Report for NM_001005242.3(PKP2):c.2176A>T (p.Thr726Ser)]
NM_001005242.3(PKP2):c.2176A>T (p.Thr726Ser)
Condition(s)
- Name:
- Arrhythmogenic right ventricular dysplasia 9 (ARVD9)
- Synonyms:
- ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9; Arrhythmogenic right ventricular cardiomyopathy, type 9; Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy 9
- Identifiers:
- MONDO: MONDO:0012180; MedGen: C1836906; OMIM: 609040
-
metagenomes
metagenomesRecovery of nearly 8,000 uncultivated bacterial and archaeal genomes substantially flesh out the tree of lifeBioProject
-
BioProject Links for SRA (Select 3800794) (1)
BioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024