Canonical Allele Identifier: PA645463132
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428809
ClinVar RCV Id: RCV000492632 RCV003766762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu169Pro
CA351756191
NM_000551.4:c.506T>C