Canonical Allele Identifier: PA916057124
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411956
ClinVar RCV Id: RCV000460540 RCV000573017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg60Gly
CA16611061
NM_198156.3:c.178C>G