Canonical Allele Identifier: PA188381
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 184253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asp545Glu
CA188379
NM_144997.7:c.1635C>G
CA398529968
NM_144997.7:c.1635C>A