Canonical Allele Identifier: PA1139756784
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 937384
ClinVar RCV Id: RCV001206380 RCV002436794 RCV003442768
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gly34Arg
CA398535336
NM_144997.7:c.100G>C
CA398535337
NM_144997.7:c.100G>A