Canonical Allele Identifier: PA2499252044
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1038449
ClinVar RCV Id: RCV001341761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val158Met
CA70046754
NM_001354723.2:c.472G>A