Canonical Allele Identifier: PA916057348
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 583075
ClinVar RCV Id: RCV000707314 RCV001016587
ClinVar Variation Id: 625232
ClinVar RCV Id: RCV000767249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Gly93Val
CA351750779
NM_198156.3:c.278G>T
CA891843322
NM_198156.3:c.278_279delinsTT