Allele Registry

Canonical Allele Identifier: PA915954366

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000823002

RCV002415942

RCV003467514

RCV004002849

ClinVar Variation:

664827

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met688Thr	CA346729169 NM_000251.3:c.2063T>C