Canonical Allele Identifier: PA2827722678
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 480818
ClinVar RCV Id: RCV000570237 RCV001352408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.His564Tyr
CA398529843
NM_001353231.2:c.1690C>T