Allele Registry

Canonical Allele Identifier: PA2827329232

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001322608

ClinVar Variation:

1022669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Ala790Glu	CA388034776 NM_001330579.2:c.2369C>A