Canonical Allele Identifier: PA2830264916
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2037757
ClinVar RCV Id: RCV002890201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.His564Gln
CA398529838
NM_144997.7:c.1692C>G
CA398529839
NM_144997.7:c.1692C>A