Canonical Allele Identifier: PA108743
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428795
ClinVar RCV Id: RCV000492520 RCV000767287 RCV000631291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu178Pro
CA351756245
NM_000551.4:c.533T>C