Canonical Allele Identifier: PA2827722615
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 819626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Thr532Pro
CA8415931
NM_001353231.2:c.1594A>C