Canonical Allele Identifier: PA2830263921
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1352848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro314Gln
CA8416191
NM_144997.7:c.941C>A