Canonical Allele Identifier: PA2827719349
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566327
ClinVar RCV Id: RCV003293577 RCV003777206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met58Thr
CA398535171
NM_001353229.2:c.173T>C