Canonical Allele Identifier: PA2825190897
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2561023
ClinVar RCV Id: RCV003300745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu63Arg
CA351748749
NM_000551.4:c.188T>G