Canonical Allele Identifier: PA108261
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2232
ClinVar RCV Id: RCV000002320 RCV000122262 RCV000148922 RCV000161094 RCV000574264 RCV000627742 RCV000722031 RCV002247239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Arg200Trp
CA020510
NM_000551.4:c.598C>T