Canonical Allele Identifier: PA1139734578
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 942411
ClinVar RCV Id: RCV001212395
ClinVar Variation Id: 2941549
ClinVar RCV Id: RCV003795251

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg172Ser
CA1139655743
NM_001354723.2:c.516G>T
CA2740090924
NM_001354723.2:c.516G>C