Canonical Allele Identifier: PA916035859
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485587
ClinVar RCV Id: RCV000562286 RCV000687129 RCV003478284
ClinVar Variation Id: 1000495
ClinVar RCV Id: RCV001296639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gly337Arg
CA8416188
NM_001353229.2:c.1009G>C
CA398532928
NM_001353229.2:c.1009G>A