Canonical Allele Identifier: PA2830430633
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456566
ClinVar RCV Id: RCV000538803 RCV002508221 RCV003302779 RCV003330751
ClinVar Variation Id: 618485
ClinVar RCV Id: RCV000756902 RCV001023281 RCV001382402
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gln123His
CA351756154
NM_198156.3:c.369G>C
CA351756157
NM_198156.3:c.369G>T