Canonical Allele Identifier: PA2827719339
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1064130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met54Ile
CA288320659
NM_001353229.2:c.162G>A
CA398535193
NM_001353229.2:c.162G>T
CA398535194
NM_001353229.2:c.162G>C