Canonical Allele Identifier: PA2827720838
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Val400Ile
CA159792
NM_001353230.2:c.1198G>A