Canonical Allele Identifier: PA2827926788
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223168
ClinVar RCV Id: RCV000679024 RCV000805326 RCV000208838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Asn78Thr
CA357095
NM_001354723.2:c.233A>C