Canonical Allele Identifier: PA108267
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2226
ClinVar RCV Id: RCV000002314 RCV000132356 RCV000208872 RCV000475973 RCV000679019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg64Pro
CA020089
NM_000551.4:c.191G>C