Canonical Allele Identifier: PA2573061944
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331792
ClinVar RCV Id: RCV001804308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly410Ala
CA346734116
NM_000251.3:c.1229G>C