Allele Registry

Canonical Allele Identifier: PA915984018

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000572927

RCV001575414

RCV001858103

RCV003320690

RCV003459289

RCV004000847

ClinVar Variation:

479788

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly42Val	CA346729713 NM_001258281.1:c.125G>T