Canonical Allele Identifier: PA116064
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006722.2:p.Phe176Ser
CA116061
NM_006731.2:c.527T>C