Canonical Allele Identifier: PA2830430948
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1687723
ClinVar RCV Id: RCV002251697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asp156Asn
CA351756524
NM_198156.3:c.466G>A