Allele Registry

Canonical Allele Identifier: PA2825279952

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000169142

ClinVar Variation:

188808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005918.1:p.Gly894Arg	CA273987 NM_001005918.3:c.2680G>A CA388028531 NM_001005918.3:c.2680G>C