Canonical Allele Identifier: PA658799989
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526685
ClinVar RCV Id: RCV000631284
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg167Leu
CA351756178
NM_000551.4:c.500G>T