Canonical Allele Identifier: PA108556
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2237
ClinVar RCV Id: RCV000002325 RCV000208813 RCV000698471 RCV002433441 RCV003460405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly93Ser
CA020230
NM_000551.4:c.277G>A