Canonical Allele Identifier: PA645426584
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gln385His
CA8416130
NM_144997.7:c.1155G>T
CA398532170
NM_144997.7:c.1155G>C