Canonical Allele Identifier: PA2827719337
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 529976
ClinVar RCV Id: RCV000635531 RCV002404768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met54Thr
CA398535196
NM_001353229.2:c.161T>C