Canonical Allele Identifier: PA916036000
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 428647
ClinVar RCV Id: RCV000492176 RCV000690635 RCV001584204 RCV002496889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Trp571Arg
CA398529920
NM_001353229.2:c.1711T>C
CA398529921
NM_001353229.2:c.1711T>A