Canonical Allele Identifier: PA2827722629
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1352071
ClinVar RCV Id: RCV002047324 RCV002388705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ile538Leu
CA398530017
NM_001353231.2:c.1612A>C