Canonical Allele Identifier: PA658669282
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 480846
ClinVar RCV Id: RCV000564563 RCV000767278 RCV001373035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Cys162_Arg167dup
CA658655759
NM_000551.4:c.483_500dup