Canonical Allele Identifier: PA164309
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 141044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp126Asn
CA020313
NM_000551.4:c.376G>A