Canonical Allele Identifier: PA2827611698
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 459217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338425.1:p.Ser352Arg
CA5170566
NM_001351496.2:c.1054A>C
CA5170567
NM_001351496.2:c.1056C>G
CA374377716
NM_001351496.2:c.1056C>A