Canonical Allele Identifier: PA1139734581
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 836162
ClinVar RCV Id: RCV001037218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly173Ser
CA916081416
NM_001354723.2:c.517G>A