Allele Registry

Canonical Allele Identifier: PA2826317770

Gene: ATP7B HGNC NCBI

ClinVar Allele:

166063

ClinVar RCV:

RCV000144367

RCV001092072

ClinVar Variation:

156283

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Arg667Gly	CA270733 NM_001243182.2:c.1999C>G