Canonical Allele Identifier: PA2827926619
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 809420
ClinVar RCV Id: RCV000997986 RCV001858871
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro40Arg
CA351747895
NM_001354723.2:c.119C>G