Canonical Allele Identifier: PA916057276
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223170
ClinVar RCV Id: RCV000631258 RCV002426981 RCV000208868 RCV003237772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Pro86Arg
CA357142
NM_198156.3:c.257C>G