Canonical Allele Identifier: PA2827720750
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1785717
ClinVar RCV Id: RCV002424029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ser360Cys
CA398532378
NM_001353230.2:c.1079C>G