Canonical Allele Identifier: PA2830430877
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 419447
ClinVar RCV Id: RCV000484822 RCV001258069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Leu143Pro
CA16617792
NM_198156.3:c.428T>C