Canonical Allele Identifier: PA2827720038
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1049988
ClinVar RCV Id: RCV001356755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ser68Asn
CA398535110
NM_001353230.2:c.203G>A