Canonical Allele Identifier: PA2827926612
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411992
ClinVar RCV Id: RCV000463141 RCV001550254 RCV002356707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly39Arg
CA039367
NM_001354723.2:c.115G>C