Canonical Allele Identifier: PA1139734516
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 967708
ClinVar RCV Id: RCV001242687
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ala168Pro
CA1139655742
NM_001354723.2:c.502G>C