Canonical Allele Identifier: PA2826317350
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 860062
ClinVar RCV Id: RCV001066306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr322Ala
CA6989381
NM_001243182.2:c.964A>G