Canonical Allele Identifier: PA2827722207
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 567047
ClinVar RCV Id: RCV000687024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Asn372Ser
CA398532298
NM_001353231.2:c.1115A>G