Canonical Allele Identifier: PA2827612586
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1054641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338427.1:p.Tyr252Phe
CA5170476
NM_001351498.2:c.755A>T