Canonical Allele Identifier: PA916057439
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 633016
ClinVar RCV Id: RCV000780788 RCV001039507
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ser111Gly
CA351751321
NM_198156.3:c.331A>G