Canonical Allele Identifier: PA2827719247
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 650505
ClinVar RCV Id: RCV000805665 RCV002268296
ClinVar Variation Id: 1030232
ClinVar RCV Id: RCV001331744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Thr18Ala
CA8416531
NM_001353229.2:c.52A>G
CA2250420706
NM_001353229.2:c.52_54delinsGCA