Canonical Allele Identifier: PA2830430908
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 182984
ClinVar RCV Id: RCV000161093 RCV000200136 RCV002345555 RCV003462112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.His150Pro
CA020500
NM_198156.3:c.449A>C