Canonical Allele Identifier: PA2827926693
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 238102
ClinVar RCV Id: RCV000230639 RCV000663291 RCV001012878 RCV002500764 RCV003151759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg58Trp
CA039640
NM_001354723.2:c.172C>T