Canonical Allele Identifier: PA2830284432
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1387371
ClinVar RCV Id: RCV001884015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Ala210Val
CA398534130
NM_144606.7:c.629C>T