Canonical Allele Identifier: PA2827722688
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 938559
ClinVar RCV Id: RCV001207804 RCV002411766 RCV002465846 RCV003478732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser567Phe
CA398529819
NM_001353231.2:c.1700C>T