Canonical Allele Identifier: PA2826317769
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3852
ClinVar RCV Id: RCV000004056 RCV000389880 RCV002444420 RCV003398441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Arg667Leu
CA340126
NM_001243182.2:c.2000G>T