Canonical Allele Identifier: PA2499251412
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1009472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Gly343Val
CA398532890
NM_001353229.2:c.1028G>T