Canonical Allele Identifier: PA2827926803
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 186220
ClinVar RCV Id: RCV000165774 RCV001388793 RCV002307423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser80Gly
CA020142
NM_001354723.2:c.238A>G