Canonical Allele Identifier: PA108540
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 496054
ClinVar RCV Id: RCV000586256 RCV001853983
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gly93Asp
CA351750781
NM_000551.4:c.278G>A