Allele Registry

Canonical Allele Identifier: PA2826464494

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000218213

RCV000629673

RCV003462501

ClinVar Variation:

232658

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val483Ile	CA10577979 NM_001258281.1:c.1447G>A