Allele Registry

Canonical Allele Identifier: PA2826463566

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000148634

RCV000222150

RCV000412467

RCV000480555

RCV000524426

RCV003997184

ClinVar Variation:

91260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser257Cys	CA022662 NM_001258281.1:c.770C>G