Canonical Allele Identifier: PA2741867960
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2944663
ClinVar RCV Id: RCV003808365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Lys162Asn
CA2740090921
NM_001354723.2:c.486A>T