Canonical Allele Identifier: PA2827926763
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 422125
ClinVar RCV Id: RCV000484327 RCV000698497 RCV002475938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val74Ala
CA16617786
NM_001354723.2:c.221T>C