Canonical Allele Identifier: PA2827328960
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495406
ClinVar RCV Id: RCV000589178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Asp681Gly
CA388021872
NM_001330579.2:c.2042A>G