Allele Registry

Canonical Allele Identifier: PA2826463112

Gene: MSH2 HGNC NCBI

ClinVar Allele:

472781

ClinVar RCV:

RCV000563062

RCV001221191

RCV004000856

ClinVar Variation:

479816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg148Gly	CA346731212 NM_001258281.1:c.442A>G