Allele Registry

Canonical Allele Identifier: PA2826465775

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001186543

ClinVar Variation:

924889

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln795Lys	CA346730997 NM_001258281.1:c.2383C>A