Canonical Allele Identifier: PA2830283932
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 950212
ClinVar RCV Id: RCV001221879 RCV001776150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Thr18Pro
CA398535428
NM_144606.7:c.52A>C