Canonical Allele Identifier: PA2827722676
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485630
ClinVar RCV Id: RCV000561170 RCV001853772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Lys562Arg
CA8415917
NM_001353231.2:c.1685A>G