Canonical Allele Identifier: PA2827612812
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 646747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338428.1:p.Asn50Ser
CA5170435
NM_001351499.2:c.149A>G