Allele Registry

Canonical Allele Identifier: PA091903

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000144365

RCV000497757

ClinVar Variation:

156281

HGVS (amino-acid)	Matching Registered Transcripts
NP_000044.2:p.Gly710Ser	CA270731 NM_000053.4:c.2128G>A