Canonical Allele Identifier: PA2827722076
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485587
ClinVar Variation Id: 1000495
ClinVar RCV Id: RCV001296639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Gly319Arg
CA8416188
NM_001353231.2:c.955G>C
CA398532928
NM_001353231.2:c.955G>A