Canonical Allele Identifier: PA108671
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428807
ClinVar RCV Id: RCV000492175 RCV000801496 RCV001702663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu118Pro
CA70049399
NM_000551.4:c.353T>C