Canonical Allele Identifier: PA2830430899
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625265
ClinVar RCV Id: RCV000767293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Leu147Gln
CA351756398
NM_198156.3:c.440T>A