Canonical Allele Identifier: PA891859224
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 579661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro311Leu
CA398532974
NM_144997.7:c.932C>T