Canonical Allele Identifier: PA1139734520
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 863831
ClinVar RCV Id: RCV001070891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ala168Val
CA896160294
NM_001354723.2:c.503C>T