Canonical Allele Identifier: PA916057238
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223169
ClinVar RCV Id: RCV000208821 RCV000803184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asn78Ile
CA357063
NM_198156.3:c.233A>T