Canonical Allele Identifier: PA1139734611
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 848432
ClinVar RCV Id: RCV001052187
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser179Thr
CA916081417
NM_001354723.2:c.535T>A