Canonical Allele Identifier: PA2827612387
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 459221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338427.1:p.Thr98Ser
CA5170365
NM_001351498.2:c.293C>G
CA374331673
NM_001351498.2:c.292A>T