Canonical Allele Identifier: PA2830263898
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1766116
ClinVar RCV Id: RCV003100117 RCV002450039 RCV003403811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu306Asp
CA398533006
NM_144997.7:c.918G>T
CA398533007
NM_144997.7:c.918G>C