Canonical Allele Identifier: PA250448
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3369
ClinVar RCV Id: RCV000003536 RCV002512711
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser79Trp
CA250446
NM_144997.7:c.236C>G