Canonical Allele Identifier: PA2827722065
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1352848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro314Gln
CA8416191
NM_001353231.2:c.941C>A