Canonical Allele Identifier: PA2580211650
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2496514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu594Gly
CA398529773
NM_001353229.2:c.1781A>G