Canonical Allele Identifier: PA1139734475
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 860843
ClinVar RCV Id: RCV001067226
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg160Pro
CA70046791
NM_001354723.2:c.479G>C