Canonical Allele Identifier: PA916075426
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 649173
ClinVar RCV Id: RCV000804045 RCV003166235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys78Arg
CA398535046
NM_144997.7:c.233A>G