Canonical Allele Identifier: PA2827722019
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2418071
ClinVar RCV Id: RCV003118180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu293Lys
CA398533109
NM_001353231.2:c.877G>A