Canonical Allele Identifier: PA1139764209
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 937122
ClinVar RCV Id: RCV001206074 RCV001586049 RCV003469335 RCV004033664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Glu12Leu
CA1139655721
NM_198156.3:c.34_35delinsTT