Canonical Allele Identifier: PA645426630
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser433Leu
CA16615110
NM_144997.7:c.1298C>T