Canonical Allele Identifier: PA658809673
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 530000
ClinVar RCV Id: RCV000635564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gly540Asp
CA398530002
NM_144997.7:c.1619G>A