Canonical Allele Identifier: PA2827926712
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 820178
ClinVar RCV Id: RCV001013381 RCV001202371
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val62Met
CA039721
NM_001354723.2:c.184G>A