Allele Registry

Canonical Allele Identifier: PA645475844

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000218052

RCV000629882

RCV001175264

RCV003997937

ClinVar Variation:

231967

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His839Asp	CA10578009 NM_000251.3:c.2515C>G