Canonical Allele Identifier: PA658680733
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile608Thr
CA346749466
NM_000179.3:c.1823T>C