Canonical Allele Identifier: PA108356
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223200
ClinVar RCV Id: RCV000208830 RCV000801501 RCV000679035 RCV004020567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp121Gly
CA357083
NM_000551.4:c.362A>G