Canonical Allele Identifier: PA658664632
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 480818
ClinVar RCV Id: RCV000570237 RCV001352408
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.His564Tyr
CA398529843
NM_144997.7:c.1690C>T