Canonical Allele Identifier: PA2826318009
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35708
ClinVar RCV Id: RCV000029357 RCV000078044 RCV001357476 RCV002433468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Arg841Lys
CA145676
NM_001243182.2:c.2522G>A