Canonical Allele Identifier: PA2827722346
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_001340160.1:p.Pro427Leu
CA288307171
NM_001353231.2:c.1280C>T