Canonical Allele Identifier: PA2580228698
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1964557
ClinVar RCV Id: RCV002740343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Cys123Ser
CA540875881
NM_001354723.2:c.367T>A
CA2580068421
NM_001354723.2:c.368G>C