Canonical Allele Identifier: PA2827720624
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 654466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala310Thr
CA8416194
NM_001353230.2:c.928G>A