Canonical Allele Identifier: PA167436
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly410Cys
CA017600
NM_000251.3:c.1228G>T