Canonical Allele Identifier: PA2827721826
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu205Pro
CA10583456
NM_001353231.2:c.614T>C