Canonical Allele Identifier: PA2827719385
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 415612
ClinVar RCV Id: RCV000461839 RCV000574441 RCV000611358 RCV001336976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Val69Ile
CA8416497
NM_001353229.2:c.205G>A