Canonical Allele Identifier: PA2825190721
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 665608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Pro45Ala
CA351748071
NM_000551.4:c.133C>G