Canonical Allele Identifier: PA2499252027
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1025978
ClinVar RCV Id: RCV001326372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ala127Asp
CA1345067194
NM_001354723.2:c.380C>A