Canonical Allele Identifier: PA2827721367
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 567066
ClinVar RCV Id: RCV000687044 RCV001556472 RCV002369833 RCV002485606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Leu29Pro
CA8416519
NM_001353231.2:c.86T>C