Canonical Allele Identifier: PA2741865178
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2681943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ile393Thr
CA398532278
NM_001353229.2:c.1178T>C