Canonical Allele Identifier: PA645463307
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 421162
ClinVar RCV Id: RCV000487120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asp197His
CA16617793
NM_000551.4:c.589G>C