Canonical Allele Identifier: PA2827926867
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1796579
ClinVar RCV Id: RCV002435110 RCV003775388
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu94Asp
CA351750796
NM_001354723.2:c.282G>C
CA351750798
NM_001354723.2:c.282G>T