Canonical Allele Identifier: PA2830264925
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1961169
ClinVar RCV Id: RCV002691157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Met566Ile
CA288303555
NM_144997.7:c.1698G>A
CA398529825
NM_144997.7:c.1698G>T
CA398529826
NM_144997.7:c.1698G>C