Canonical Allele Identifier: PA645463317
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411984
ClinVar RCV Id: RCV000467837 RCV002356705 RCV003153642 RCV003463964 RCV003480645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Thr202Ile
CA041863
NM_000551.4:c.605C>T