Canonical Allele Identifier: PA2827926953
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411987
ClinVar RCV Id: RCV000467414 RCV003230506 RCV002451138 RCV004001992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg113Pro
CA040338
NM_001354723.2:c.338G>C