Canonical Allele Identifier: PA2830263901
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 853577
ClinVar RCV Id: RCV001058413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu307Lys
CA398533005
NM_144997.7:c.919G>A