Canonical Allele Identifier: PA645426421
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 415612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Val69Ile
CA8416497
NM_144997.7:c.205G>A