Canonical Allele Identifier: PA2827721279
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 944338
ClinVar RCV Id: RCV001214711 RCV002402638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala574Val
CA398529784
NM_001353230.2:c.1721C>T