Canonical Allele Identifier: PA2827722183
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Phe361Ser
CA398532372
NM_001353231.2:c.1082T>C