Canonical Allele Identifier: PA2827722717
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2496514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu576Gly
CA398529773
NM_001353231.2:c.1727A>G