Canonical Allele Identifier: PA2826464394
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg458Gly
CA346727825
NM_001258281.1:c.1372C>G