Canonical Allele Identifier: PA2827722056
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 959113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro311Arg
CA288311750
NM_001353231.2:c.932C>G