Canonical Allele Identifier: PA2830430925
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1932822
ClinVar RCV Id: RCV002635553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gln154Pro
CA351756493
NM_198156.3:c.461A>C