Canonical Allele Identifier: PA916057442
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223186
ClinVar RCV Id: RCV000208834 RCV000492721 RCV002517414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ser111Asn
CA357091
NM_198156.3:c.332G>A