Canonical Allele Identifier: PA1139764246
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 945878
ClinVar RCV Id: RCV001216618 RCV002375187
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly30Trp
CA351747567
NM_198156.3:c.88G>T