Canonical Allele Identifier: PA2827719398
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1345154
ClinVar RCV Id: RCV002034963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro74Gln
CA398535070
NM_001353229.2:c.221C>A