Canonical Allele Identifier: PA2580211621
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1776825
ClinVar RCV Id: RCV002401283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu562Lys
CA398529982
NM_001353229.2:c.1684G>A