Canonical Allele Identifier: PA2827614019
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 459217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338431.1:p.Ser220Arg
CA5170566
NM_001351502.2:c.658A>C
CA5170567
NM_001351502.2:c.660C>G
CA374377716
NM_001351502.2:c.660C>A