Canonical Allele Identifier: PA2827721184
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2905593
ClinVar RCV Id: RCV003607055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu530Val
CA398530424
NM_001353230.2:c.1589A>T