Canonical Allele Identifier: PA916035880
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met381Leu
CA398532361
NM_001353229.2:c.1141A>T
CA398532363
NM_001353229.2:c.1141A>C