Canonical Allele Identifier: PA2826318121
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 558616
ClinVar RCV Id: RCV000674914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Val913Ala
CA388030735
NM_001243182.2:c.2738T>C