Canonical Allele Identifier: PA891859241
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 574519
ClinVar RCV Id: RCV000696473
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Cys415Arg
CA398531776
NM_144997.7:c.1243T>C