Canonical Allele Identifier: PA2830430898
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 625266
ClinVar RCV Id: RCV000767294 RCV002536595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Leu147Pro
CA351756399
NM_198156.3:c.440T>C