Canonical Allele Identifier: PA116083
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006722.2:p.Ala170Glu
CA116080
NM_006731.2:c.509C>A