Canonical Allele Identifier: PA2499252032
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1015452
ClinVar RCV Id: RCV001314314
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Asn131Asp
CA1345067219
NM_001354723.2:c.391A>G