Canonical Allele Identifier: PA2827926645
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 648726
ClinVar RCV Id: RCV000803524 RCV003238229 RCV004001665 RCV002381760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro45Leu
CA70042375
NM_001354723.2:c.134C>T