Canonical Allele Identifier: PA2827926577
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 968522
ClinVar RCV Id: RCV001243676 RCV004034759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu31Asp
CA351747611
NM_001354723.2:c.93G>C
CA351747615
NM_001354723.2:c.93G>T