Canonical Allele Identifier: PA2830264227
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2000398
ClinVar RCV Id: RCV002824500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Phe388Leu
CA398532134
NM_144997.7:c.1164T>G
CA398532135
NM_144997.7:c.1164T>A
CA398532145
NM_144997.7:c.1162T>C