Canonical Allele Identifier: PA2830283938
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460621
ClinVar RCV Id: RCV000535153 RCV000562808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Phe20Tyr
CA398535414
NM_144606.7:c.59T>A