Allele Registry

Canonical Allele Identifier: PA2827326664

Gene: ATP7B HGNC NCBI

ClinVar Allele:

358221

ClinVar RCV:

RCV000410034

ClinVar Variation:

370820

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Gly1021Ser	CA6988744 NM_001330578.2:c.3061G>A