Canonical Allele Identifier: PA2827719697
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3229221
ClinVar RCV Id: RCV004524800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Cys353Gly
CA398532810
NM_001353229.2:c.1057T>G