Canonical Allele Identifier: PA916035812
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485580
ClinVar RCV Id: RCV000560997 RCV001059272 RCV002491135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala243Thr
CA8416341
NM_001353229.2:c.727G>A