Canonical Allele Identifier: PA2825279699
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_001005918.1:p.Val728Met
CA274401
NM_001005918.3:c.2182G>A