Canonical Allele Identifier: PA2827722014
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 822698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Asp291Glu
CA398533116
NM_001353231.2:c.873T>G
CA398533117
NM_001353231.2:c.873T>A