Canonical Allele Identifier: PA2827611928
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1363243
ClinVar RCV Id: RCV001934814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338426.1:p.Pro136Ala
CA374332076
NM_001351497.2:c.406C>G