Canonical Allele Identifier: PA159794
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134431
ClinVar RCV Id: RCV000121111 RCV000166127 RCV000231168
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Val400Ile
CA159792
NM_144997.7:c.1198G>A