Canonical Allele Identifier: PA2826231009
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 407110
ClinVar RCV Id: RCV000477010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185892.1:p.Asp196Tyr
CA5170441
NM_001198963.2:c.586G>T