Canonical Allele Identifier: PA2826317579
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075306
ClinVar RCV Id: RCV004015832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.His529Arg
CA388027568
NM_001243182.2:c.1586A>G