Allele Registry

Canonical Allele Identifier: PA2827329428

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000169455

RCV001531800

ClinVar Variation:

189058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Gly859Asp	CA274329 NM_001330579.2:c.2576G>A