Canonical Allele Identifier: PA2579915610
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1754638
ClinVar RCV Id: RCV002366800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln409His
CA346734100
NM_000251.3:c.1227G>C
CA346734102
NM_000251.3:c.1227G>T