Canonical Allele Identifier: PA2826463948
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2848775
ClinVar RCV Id: RCV003758568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly344Asp
CA346734111
NM_001258281.1:c.1031G>A