Allele Registry

Canonical Allele Identifier: PA2826465676

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000218052

RCV000629882

RCV001175264

RCV003997937

ClinVar Variation:

231967

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.His773Asp	CA10578009 NM_001258281.1:c.2317C>G