Canonical Allele Identifier: PA2830430881
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223232
ClinVar RCV Id: RCV000208797 RCV000236099 RCV000565491 RCV000631260 RCV002485365 RCV003422117 RCV003462397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Tyr144Cys
CA041601
NM_198156.3:c.431A>G