Allele Registry

Canonical Allele Identifier: PA2827330391

Gene: ATP7B HGNC NCBI

ClinVar Allele:

167803

ClinVar RCV:

RCV000145281

RCV003895025

ClinVar Variation:

157956

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Gly1263Ser	CA271178 NM_001330579.2:c.3787G>A