Canonical Allele Identifier: PA159791
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 134430
ClinVar RCV Id: RCV000121110 RCV000568600 RCV000635530 RCV002483217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Pro428Leu
CA159789
NM_144997.7:c.1283C>T