Canonical Allele Identifier: PA2827611979
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1021038
ClinVar RCV Id: RCV001320727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338426.1:p.Leu166Phe
CA197437854
NM_001351497.2:c.498G>T
CA374332272
NM_001351497.2:c.498G>C