Canonical Allele Identifier: PA2573205661
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1503291
ClinVar RCV Id: RCV002022745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly173Asp
CA2573136133
NM_001354723.2:c.518G>A