Canonical Allele Identifier: PA2573205663
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1392090
ClinVar RCV Id: RCV001896047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly175Ser
CA2573136134
NM_001354723.2:c.523G>A