Canonical Allele Identifier: PA2827721214
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 184253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Asp545Glu
CA188379
NM_001353230.2:c.1635C>G
CA398529968
NM_001353230.2:c.1635C>A