Canonical Allele Identifier: PA2826318290
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 550770
ClinVar RCV Id: RCV000665607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Arg1040Gly
CA388026626
NM_001243182.2:c.3118C>G