Canonical Allele Identifier: PA2827722251
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1487995
ClinVar RCV Id: RCV002008994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Thr393Ala
CA398532030
NM_001353231.2:c.1177A>G