Canonical Allele Identifier: PA2826230992
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 646747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185892.1:p.Asn182Ser
CA5170435
NM_001198963.2:c.545A>G