Canonical Allele Identifier: PA658664355
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460621
ClinVar RCV Id: RCV000535153 RCV000562808
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Phe20Tyr
CA398535414
NM_144997.7:c.59T>A