Canonical Allele Identifier: PA2826463941
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1754273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln343Arg
CA346734095
NM_001258281.1:c.1028A>G