Canonical Allele Identifier: PA2827722320
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 253246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu418Pro
CA10586257
NM_001353231.2:c.1253T>C