Canonical Allele Identifier: PA658669301
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 486713
ClinVar RCV Id: RCV000569840 RCV001210329 RCV002483543 RCV003322793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Val170Ile
CA351756194
NM_000551.4:c.508G>A