Canonical Allele Identifier: PA2827719748
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229227
ClinVar RCV Id: RCV004524806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Cys433Tyr
CA398531772
NM_001353229.2:c.1298G>A