Canonical Allele Identifier: PA2827926709
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 947545
ClinVar RCV Id: RCV001218645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val62Glu
CA351748739
NM_001354723.2:c.185T>A