Canonical Allele Identifier: PA189482
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 184619
ClinVar RCV Id: RCV000163906 RCV000529447 RCV001544699 RCV002492651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro428His
CA189480
NM_144997.7:c.1283C>A