Canonical Allele Identifier: PA2827719289
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 230017
ClinVar RCV Id: RCV000222636 RCV000635568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Asp33Tyr
CA10580176
NM_001353229.2:c.97G>T