Allele Registry

Canonical Allele Identifier: PA915983962

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001018072

RCV001585923

ClinVar Variation:

822597

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu35Lys	CA346729627 NM_001258281.1:c.103G>A