Canonical Allele Identifier: PA2827721900
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 253233
ClinVar RCV Id: RCV000239701 RCV000561577 RCV001527887 RCV002487112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg239His
CA8416333
NM_001353231.2:c.716G>A