Canonical Allele Identifier: PA2827926714
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2227
ClinVar RCV Id: RCV000002315 RCV000585971 RCV000704785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Leu63Pro
CA020079
NM_001354723.2:c.188T>C