Canonical Allele Identifier: PA916031060
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338426.1:p.Ala91Thr
CA116076
NM_001351497.2:c.271G>A