Canonical Allele Identifier: PA2830263955
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 658315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gln324Arg
CA8416186
NM_144997.7:c.971A>G