Canonical Allele Identifier: PA2827720462
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229258
ClinVar RCV Id: RCV004524837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly235Asp
CA398533965
NM_001353230.2:c.704G>A