Canonical Allele Identifier: PA2827722697
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 229915
ClinVar RCV Id: RCV000213870 RCV000701876 RCV001555199 RCV002494583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg570His
CA8415911
NM_001353231.2:c.1709G>A