Allele Registry

Canonical Allele Identifier: PA2825279948

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000410034

ClinVar Variation:

370820

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005918.1:p.Gly892Ser	CA6988744 NM_001005918.3:c.2674G>A