Canonical Allele Identifier: PA1139737591
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 840448
ClinVar RCV Id: RCV001042440 RCV002348358 RCV003442156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Val402Ile
CA8416132
NM_001353229.2:c.1204G>A