Canonical Allele Identifier: PA2827722075
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 530001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu318Lys
CA8416189
NM_001353231.2:c.952G>A