Canonical Allele Identifier: PA645463194
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 419861
ClinVar RCV Id: RCV000705398 RCV001704601 RCV002350061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp179Asn
CA041455
NM_000551.4:c.535G>A