Canonical Allele Identifier: PA916057309
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 633017
ClinVar RCV Id: RCV000780789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asn90Tyr
CA351750702
NM_198156.3:c.268A>T