Canonical Allele Identifier: PA2579915618
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2848775
ClinVar RCV Id: RCV003758568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly410Asp
CA346734111
NM_000251.3:c.1229G>A