Allele Registry

Canonical Allele Identifier: PA1139682118

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001186543

ClinVar Variation:

924889

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln861Lys	CA346730997 NM_000251.3:c.2581C>A