Allele Registry

Canonical Allele Identifier: PA645470996

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000226454

RCV000664273

RCV001658053

RCV002282071

RCV003998766

ClinVar Variation:

237411

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Pro27Thr	CA10581989 NM_000251.3:c.79C>A