Allele Registry

Canonical Allele Identifier: PA2826318086

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000145267

ClinVar Variation:

157943

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gln893Pro	CA271174 NM_001243182.2:c.2678A>C