Canonical Allele Identifier: PA916035921
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 566387
ClinVar RCV Id: RCV000686185 RCV001010727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro445Leu
CA288307171
NM_001353229.2:c.1334C>T