Canonical Allele Identifier: PA2827721398
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1505643
ClinVar RCV Id: RCV001999558
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Gly40Val
CA398535290
NM_001353231.2:c.119G>T