Canonical Allele Identifier: PA916035833
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322066
ClinVar RCV Id: RCV000293686 RCV000348649 RCV001556414 RCV002418183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala282Val
CA8416291
NM_001353229.2:c.845C>T