Canonical Allele Identifier: PA891859231
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 567047
ClinVar RCV Id: RCV000687024
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asn372Ser
CA398532298
NM_144997.7:c.1115A>G