Allele Registry

Canonical Allele Identifier: PA2827327292

Gene: ATP7B HGNC NCBI

ClinVar Allele:

167802

ClinVar RCV:

RCV000145280

ClinVar Variation:

157955

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Gly1263Ser	CA271177 NM_001330578.2:c.3787G>A