Canonical Allele Identifier: PA2827722713
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1059893
ClinVar RCV Id: RCV001369254 RCV002413884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Ser575Leu
CA8415908
NM_001353231.2:c.1724C>T