Canonical Allele Identifier: PA2827613498
Gene: FKTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2089208
ClinVar RCV Id: RCV003012033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338430.1:p.Ser10Arg
CA374331975
NM_001351501.2:c.28A>C
CA374331978
NM_001351501.2:c.30T>A
CA374331979
NM_001351501.2:c.30T>G