Canonical Allele Identifier: PA2825279891
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 550969
ClinVar RCV Id: RCV000665883 RCV001508709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Glu857Lys
CA6988782
NM_001005918.3:c.2569G>A