Canonical Allele Identifier: PA2827721175
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg527Gln
CA8415934
NM_001353230.2:c.1580G>A