Canonical Allele Identifier: PA2580211636
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_001340158.1:p.His582Gln
CA398529838
NM_001353229.2:c.1746C>G
CA398529839
NM_001353229.2:c.1746C>A