Canonical Allele Identifier: PA2827612766
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338428.1:p.Gly17Arg
CA5170415
NM_001351499.2:c.49G>A
CA374332014
NM_001351499.2:c.49G>C