Allele Registry

Canonical Allele Identifier: PA658736036

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.8112036712

ClinVar RCV:

RCV000580643

RCV001038381

ClinVar Variation:

489927

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val63Leu	CA346729017 NM_000251.3:c.187G>C CA346729018 NM_000251.3:c.187G>T