Canonical Allele Identifier: PA2826230887
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1498251
ClinVar RCV Id: RCV002019612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185892.1:p.Pro107Ala
CA374331731
NM_001198963.2:c.319C>G