Canonical Allele Identifier: PA2830264174
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2578502
ClinVar RCV Id: RCV003326278
ClinVar Variation Id: 2972839
ClinVar RCV Id: RCV003837949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Trp376Arg
CA398532274
NM_144997.7:c.1126T>C
CA398532275
NM_144997.7:c.1126T>A