Canonical Allele Identifier: PA1139737662
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 860539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.His441Gln
CA398531676
NM_001353229.2:c.1323C>A
CA398531678
NM_001353229.2:c.1323C>G