Canonical Allele Identifier: PA2827720007
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 576689
ClinVar RCV Id: RCV000699243 RCV001012686 RCV002268258 RCV003332237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg57Trp
CA8416510
NM_001353230.2:c.169C>T