Allele Registry

Canonical Allele Identifier: PA2826318512

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000169572

ClinVar Variation:

189149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Leu1188Phe	CA274423 NM_001243182.2:c.3562C>T