Canonical Allele Identifier: PA2830430774
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_937799.1:p.Asn133Tyr
CA16611095
NM_198156.3:c.397A>T