Canonical Allele Identifier: PA658664365
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ala45Val
CA8416512
NM_144997.7:c.134C>T