Allele Registry

Canonical Allele Identifier: PA658736319

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000588121

RCV004002417

ClinVar Variation:

495771

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln160Lys	CA346730592 NM_000251.3:c.478C>A