Canonical Allele Identifier: PA645462961
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411970
ClinVar RCV Id: RCV000462284 RCV000479517 RCV000708764 RCV002272247 RCV002489086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.His125Tyr
CA040676
NM_000551.4:c.373C>T