Canonical Allele Identifier: PA658799974
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526672
ClinVar RCV Id: RCV000631266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Val142Ala
CA351754163
NM_000551.4:c.425T>C