Canonical Allele Identifier: PA2830284020
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1064130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Met54Ile
CA288320659
NM_144606.7:c.162G>A
CA398535193
NM_144606.7:c.162G>T
CA398535194
NM_144606.7:c.162G>C