Canonical Allele Identifier: PA357122
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223214
ClinVar RCV Id: RCV000208855 RCV001853329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ala149Pro
CA357120
NM_000551.4:c.445G>C