Canonical Allele Identifier: PA2827719936
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 949189
ClinVar RCV Id: RCV001220594 RCV002447108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Leu29His
CA398535362
NM_001353230.2:c.86T>A