Canonical Allele Identifier: PA2826318504
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 161207
ClinVar RCV Id: RCV000148375 RCV001091634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Asp1185Asn
CA272855
NM_001243182.2:c.3553G>A