Canonical Allele Identifier: PA1139734487
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 849597
ClinVar RCV Id: RCV001053601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Leu166Arg
CA916081415
NM_001354723.2:c.497T>G