Canonical Allele Identifier: PA2830264767
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1026891
ClinVar RCV Id: RCV001327412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Val524Gly
CA398530463
NM_144997.7:c.1571T>G