Canonical Allele Identifier: PA2827719331
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586498
ClinVar RCV Id: RCV003360556
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gly51Val
CA398535215
NM_001353229.2:c.152G>T