Canonical Allele Identifier: PA2827926661
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 935622
ClinVar RCV Id: RCV001204260
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ala50Gly
CA351748259
NM_001354723.2:c.149C>G