Allele Registry

Canonical Allele Identifier: PA2826465868

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000566548

ClinVar Variation:

480959

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu815Lys	CA346731335 NM_001258281.1:c.2443G>A