NM_147127.5(EVC2):c.2668G>A (p.Val890Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002557129.2
Allele description [Variation Report for NM_147127.5(EVC2):c.2668G>A (p.Val890Met)]
NM_147127.5(EVC2):c.2668G>A (p.Val890Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Sequence 11 from Patent WO9405786
Sequence 11 from Patent WO9405786gi|2294432|emb|A37570.1||pat|WO|940 11Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024