Allele Registry

Canonical Allele Identifier: PA2826463875

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000231260

RCV001183558

ClinVar Variation:

237360

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys327Gln	CA10582009 NM_001258281.1:c.979A>C