Allele Registry

Canonical Allele Identifier: PA287462

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115537

RCV000196378

RCV000215932

RCV000411245

RCV002360225

RCV002505033

RCV003997281

ClinVar Variation:

127648

1751677

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly204Arg	CA021573 NM_000251.3:c.610G>A CA346731092 NM_000251.3:c.610G>C