Canonical Allele Identifier: PA2827720584
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485619
ClinVar RCV Id: RCV000564905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Asp291Gly
CA398533119
NM_001353230.2:c.872A>G