Canonical Allele Identifier: PA916057265
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428813
ClinVar RCV Id: RCV000492467 RCV000631269 RCV000767245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Val84Met
CA351750580
NM_198156.3:c.250G>A