Canonical Allele Identifier: PA2827721233
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 428647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Trp553Arg
CA398529920
NM_001353230.2:c.1657T>C
CA398529921
NM_001353230.2:c.1657T>A