Canonical Allele Identifier: PA2499252049
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1023770
ClinVar RCV Id: RCV001323871 RCV001810030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg160His
CA896160287
NM_001354723.2:c.479G>A