Canonical Allele Identifier: PA2827926656
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1018990
ClinVar RCV Id: RCV001318363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly49Val
CA351748222
NM_001354723.2:c.146G>T