Canonical Allele Identifier: PA096882
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073270.1:p.Arg307Gln
CA116072
NM_001079802.2:c.920G>A