Canonical Allele Identifier: PA2826463262
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1697891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu185Gly
CA346732328
NM_001258281.1:c.554A>G