Canonical Allele Identifier: PA2827720411
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gln212Lys
CA8416347
NM_001353230.2:c.634C>A