Allele Registry

Canonical Allele Identifier: PA2826318138

Gene: ATP7B HGNC NCBI

ClinVar Allele:

358223

ClinVar RCV:

RCV000410994

ClinVar Variation:

371021

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gly924Val	CA16041666 NM_001243182.2:c.2771G>T