Canonical Allele Identifier: PA2825085428
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1684897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg58Thr
CA346735000
NM_000179.3:c.173G>C