Canonical Allele Identifier: PA108837
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 182979
ClinVar RCV Id: RCV000161087 RCV000208869 RCV000817709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu89Pro
CA020207
NM_000551.4:c.266T>C