Canonical Allele Identifier: PA916056883
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411971
ClinVar RCV Id: RCV000471735 RCV002436462
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Asp9Ala
CA16611161
NM_198156.3:c.26A>C