Canonical Allele Identifier: PA2827722056
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 959113
ClinVar RCV Id: RCV001232402 RCV002375239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Pro311Arg
CA288311750
NM_001353231.2:c.932C>G