Allele Registry

Canonical Allele Identifier: PA2827329799

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000411980

RCV001508707

ClinVar Variation:

371498

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Val1022Asp	CA6988740 NM_001330579.2:c.3065T>A