Canonical Allele Identifier: PA2827926804
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625229
ClinVar RCV Id: RCV000767244 RCV001220559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser80Ile
CA16621914
NM_001354723.2:c.239G>T