Canonical Allele Identifier: PA096913
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3204
ClinVar RCV Id: RCV000003358 RCV000626166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073270.1:p.Phe176Ser
CA116061
NM_001079802.2:c.527T>C