Canonical Allele Identifier: PA162665
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 135406
ClinVar RCV Id: RCV000122260 RCV000409700 RCV000492595 RCV000467198 RCV000657025 RCV002483231
ClinVar Variation Id: 238106
ClinVar RCV Id: RCV000228663 RCV000236708 RCV000411808 RCV000562501 RCV002307459 RCV002487052
ClinVar Variation Id: 582995
ClinVar RCV Id: RCV000707210 RCV002369974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Met1Ile