Canonical Allele Identifier: PA2827326090
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 189121
ClinVar RCV Id: RCV000169535 RCV000514615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val812Met
CA274401
NM_001330578.2:c.2434G>A