Canonical Allele Identifier: PA645462961
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.His125Tyr
CA040676
NM_000551.4:c.373C>T