Canonical Allele Identifier: PA2830264861
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1041689
ClinVar RCV Id: RCV001345530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys548Thr
CA398529951
NM_144997.7:c.1643A>C