Canonical Allele Identifier: PA2827719402
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1369394
ClinVar RCV Id: RCV001870603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro74Arg
CA398535071
NM_001353229.2:c.221C>G