Allele Registry

Canonical Allele Identifier: PA2579910400

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001018072

RCV001585923

ClinVar Variation:

822597

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu101Lys	CA346729627 NM_000251.3:c.301G>A