Canonical Allele Identifier: PA645462669
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 371800
ClinVar RCV Id: RCV000409162 RCV000782251 RCV002481266 RCV000530730 RCV001012691 RCV003470356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala56Gly
CA039566
NM_000551.4:c.167C>G