Canonical Allele Identifier: PA1139737543
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 946391
ClinVar RCV Id: RCV001217252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala376Thr
CA398532390
NM_001353229.2:c.1126G>A