Canonical Allele Identifier: PA658669245
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 456585
ClinVar RCV Id: RCV000553383 RCV001021117 RCV001764530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp126Gly
CA351753841
NM_000551.4:c.377A>G