Allele Registry

Canonical Allele Identifier: PA2826318452

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV002248978

ClinVar Variation:

1685251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Asn1159Ile	CA6988565 NM_001243182.2:c.3476A>T