Canonical Allele Identifier: PA916035849
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529990
ClinVar RCV Id: RCV000635550
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser320Cys
CA398533036
NM_001353229.2:c.959C>G