Canonical Allele Identifier: PA2499252056
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1053429
ClinVar RCV Id: RCV001361771
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly173Ala
CA2499216369
NM_001354723.2:c.518G>C