Canonical Allele Identifier: PA645463136
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411983
ClinVar RCV Id: RCV000461022 RCV003298509 RCV004001990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Asn174Tyr
CA16611095
NM_000551.4:c.520A>T