Canonical Allele Identifier: PA2827720655
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 658315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gln324Arg
CA8416186
NM_001353230.2:c.971A>G