Canonical Allele Identifier: PA2827719874
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 940936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Val5Met
CA8416539
NM_001353230.2:c.13G>A