Canonical Allele Identifier: PA2827926871
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 576054
ClinVar RCV Id: RCV000698452 RCV003106023 RCV003338740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro95Leu
CA70046204
NM_001354723.2:c.284C>T