Canonical Allele Identifier: PA096922
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073270.1:p.Tyr371Cys
CA116084
NM_001079802.2:c.1112A>G