Canonical Allele Identifier: PA2830430974
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 421558
ClinVar RCV Id: RCV000479035 RCV000823835 RCV001143974 RCV001024771 RCV003464021 RCV003401545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg159Gln
CA041791
NM_198156.3:c.476G>A