Canonical Allele Identifier: PA916035923
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 184619
ClinVar RCV Id: RCV000163906 RCV000529447 RCV001544699 RCV002492651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro446His
CA189480
NM_001353229.2:c.1337C>A