Canonical Allele Identifier: PA2827926725
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 547829
ClinVar RCV Id: RCV000660351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser65Pro
CA351748798
NM_001354723.2:c.193T>C