Canonical Allele Identifier: PA2499251444
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1054815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Tyr423His
CA398531900
NM_001353229.2:c.1267T>C