Canonical Allele Identifier: PA2830283918
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2803549
ClinVar RCV Id: RCV003607771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Gly15Val
CA398535440
NM_144606.7:c.44G>T