Canonical Allele Identifier: PA2741815428
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2946037
ClinVar RCV Id: RCV003806323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Ile180Leu
CA351756270
NM_000551.4:c.538A>C