Canonical Allele Identifier: PA2827722591
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 653093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Lys520Arg
CA8415935
NM_001353231.2:c.1559A>G