Canonical Allele Identifier: PA357045
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn90Ile
CA357043
NM_000551.4:c.269A>T