Canonical Allele Identifier: PA2827719426
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1062664
ClinVar RCV Id: RCV001372406 RCV002447492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Cys82Tyr
CA398535018
NM_001353229.2:c.245G>A