Allele Registry

Canonical Allele Identifier: PA2825280135

Gene: ATP7B HGNC NCBI

ClinVar Allele:

18898

ClinVar RCV:

RCV000004063

RCV000595271

RCV002354147

RCV003904803

ClinVar Variation:

3859

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005918.1:p.Asn1063Ser	CA252896 NM_001005918.3:c.3188A>G