Canonical Allele Identifier: PA2827719228
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1722109
ClinVar RCV Id: RCV002295154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Glu12Gly
CA398535460
NM_001353229.2:c.35A>G