Canonical Allele Identifier: PA159800
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134432
ClinVar RCV Id: RCV000121113 RCV000535074 RCV000573718 RCV001562933 RCV002492423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg350Gln
CA159798
NM_144997.7:c.1049G>A