Canonical Allele Identifier: PA2830284082
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1369394
ClinVar RCV Id: RCV001870603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Pro74Arg
CA398535071
NM_144606.7:c.221C>G