Canonical Allele Identifier: PA2827722036
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu303Gly
CA8416196
NM_001353231.2:c.908A>G