Canonical Allele Identifier: PA2827719988
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 640135
ClinVar RCV Id: RCV000793095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly50Asp
CA398535223
NM_001353230.2:c.149G>A