Canonical Allele Identifier: PA2827722698
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 819901
ClinVar RCV Id: RCV001012834 RCV001242710 RCV003493773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg570Cys
CA8415912
NM_001353231.2:c.1708C>T