Allele Registry

Canonical Allele Identifier: PA2826465338

Gene: MSH2 HGNC NCBI

ClinVar Allele:

472874

ClinVar RCV:

RCV000561848

RCV001065224

RCV003987610

ClinVar Variation:

483667

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile681Val	CA346729739 NM_001258281.1:c.2041A>G