Canonical Allele Identifier: PA2827926667
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 840866
ClinVar RCV Id: RCV001042972 RCV004031308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu51Gln
CA351748282
NM_001354723.2:c.151G>C