Allele Registry

Canonical Allele Identifier: PA658672395

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000567509

RCV000685208

RCV000759100

RCV003459384

RCV004001116

ClinVar Variation:

485825

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met460Thr	CA346724826 NM_000251.3:c.1379T>C