Canonical Allele Identifier: PA108664
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 428802
ClinVar RCV Id: RCV000492280 RCV003233031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Leu118Arg
CA351753694
NM_000551.4:c.353T>G