Allele Registry

Canonical Allele Identifier: PA2827329186

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000670079

RCV001509442

ClinVar Variation:

554444

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Thr766Ile	CA6988979 NM_001330579.2:c.2297C>T