Canonical Allele Identifier: PA2827720646
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485587
ClinVar RCV Id: RCV000562286 RCV000687129 RCV003478284
ClinVar Variation Id: 1000495
ClinVar RCV Id: RCV001296639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly319Arg
CA8416188
NM_001353230.2:c.955G>C
CA398532928
NM_001353230.2:c.955G>A