Canonical Allele Identifier: PA2827926554
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411976
ClinVar RCV Id: RCV000465780 RCV002383832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro25Ala
CA042053
NM_001354723.2:c.73C>G