Canonical Allele Identifier: PA2741865331
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2830381
ClinVar RCV Id: RCV003608070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Phe570Leu
CA398529922
NM_001353229.2:c.1710C>G
CA398529923
NM_001353229.2:c.1710C>A
CA398529928
NM_001353229.2:c.1708T>C