Canonical Allele Identifier: PA658664460
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485619
ClinVar RCV Id: RCV000564905
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asp291Gly
CA398533119
NM_144997.7:c.872A>G