Canonical Allele Identifier: PA2827720398
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Leu205Pro
CA10583456
NM_001353230.2:c.614T>C