Canonical Allele Identifier: PA916031078
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 435193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338431.1:p.Ala38Thr
CA5170425
NM_001351502.2:c.112G>A