Canonical Allele Identifier: PA2499252046
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1056712
ClinVar RCV Id: RCV001365585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Trp159Gly
CA2499216365
NM_001354723.2:c.475T>G