Allele Registry

Canonical Allele Identifier: PA091879

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000410034

ClinVar Variation:

370820

HGVS (amino-acid)	Matching Registered Transcripts
NP_000044.2:p.Gly1099Ser	CA6988744 NM_000053.4:c.3295G>A