NM_020381.4(PDSS2):c.635T>C (p.Val212Ala) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004068711.1
Allele description [Variation Report for NM_020381.4(PDSS2):c.635T>C (p.Val212Ala)]
NM_020381.4(PDSS2):c.635T>C (p.Val212Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
SRX1471767 (1)
SRA
-
tmtc2a [Onychostoma macrolepis]
tmtc2a [Onychostoma macrolepis]Gene ID:131539566Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024