Canonical Allele Identifier: PA2827722185
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566338
ClinVar RCV Id: RCV003293583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg362Ser
CA398532367
NM_001353231.2:c.1084C>A