Canonical Allele Identifier: PA332652
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135953
ClinVar RCV Id: RCV000123104 RCV000524493 RCV001657771 RCV002426672 RCV003460872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp9Asn
CA020190
NM_000551.4:c.25G>A