Canonical Allele Identifier: PA2827720657
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1009472
ClinVar RCV Id: RCV001306966 RCV002384378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gly325Val
CA398532890
NM_001353230.2:c.974G>T