Canonical Allele Identifier: PA2827721267
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1043559
ClinVar RCV Id: RCV001347686 RCV002404819 RCV002493791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg570Leu
CA288303537
NM_001353230.2:c.1709G>T