Canonical Allele Identifier: PA108487
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 161402
ClinVar RCV Id: RCV000148923 RCV000575111 RCV000227809 RCV001704076 RCV001843484 RCV002465537 RCV002467589 RCV003415985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu52Lys
CA020056
NM_000551.4:c.154G>A