Canonical Allele Identifier: PA2826317997
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_001230111.1:p.Gly832Ser
CA252894
NM_001243182.2:c.2494G>A