Canonical Allele Identifier: PA2827719992
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586498
ClinVar RCV Id: RCV003360556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly51Val
CA398535215
NM_001353230.2:c.152G>T