Canonical Allele Identifier: PA2830283982
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2123091
ClinVar RCV Id: RCV003054905 RCV003274163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Asp37Gly
CA398535311
NM_144606.7:c.110A>G