Canonical Allele Identifier: PA2830264273
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 639998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg401His
CA8416095
NM_144997.7:c.1202G>A