Allele Registry

Canonical Allele Identifier: PA2826465160

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000221209

RCV000479697

RCV000553991

RCV003997901

ClinVar Variation:

231482

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu635Ala	CA10577998 NM_001258281.1:c.1904A>C