Canonical Allele Identifier: PA2580521701
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1914727
ClinVar RCV Id: RCV002612812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Gly51Asp
CA398535217
NM_144997.7:c.152G>A