Canonical Allele Identifier: PA2827926760
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 651175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gln73His
CA351749148
NM_001354723.2:c.219G>C
CA351749151
NM_001354723.2:c.219G>T