Canonical Allele Identifier: PA916035860
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 645979
ClinVar RCV Id: RCV000800171 RCV002386417 RCV003442084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg338Trp
CA8416187
NM_001353229.2:c.1012C>T