Allele Registry

Canonical Allele Identifier: PA2826462804

Gene: MSH2 HGNC NCBI

ClinVar Allele:

232522

ClinVar RCV:

RCV000215101

RCV000227027

RCV001030705

RCV001532987

RCV003997972

ClinVar Variation:

232406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Val23Ala	CA10577929 NM_001258281.1:c.68T>C