Canonical Allele Identifier: PA2827329425
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3856
ClinVar RCV Id: RCV000004060 RCV001091638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly859Ser
CA252894
NM_001330579.2:c.2575G>A