Canonical Allele Identifier: PA2827926861
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 496054
ClinVar RCV Id: RCV000586256 RCV001853983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly93Asp
CA351750781
NM_001354723.2:c.278G>A