Canonical Allele Identifier: PA2827926844
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 633017
ClinVar RCV Id: RCV000780789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Asn90Tyr
CA351750702
NM_001354723.2:c.268A>T