Canonical Allele Identifier: PA645426646
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322062
ClinVar RCV Id: RCV000321128 RCV000375788 RCV000571724
ClinVar Variation Id: 2445313
ClinVar RCV Id: RCV003154723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asp476Glu
CA8416006
NM_144997.7:c.1428C>G
CA398531084
NM_144997.7:c.1428C>A