Canonical Allele Identifier: PA2825190778
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 661344
ClinVar RCV Id: RCV000818739 RCV002390679 RCV003413650 RCV004001814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Glu51Lys
CA351748278
NM_000551.4:c.151G>A