Allele Registry

Canonical Allele Identifier: PA915955088

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001852911

ClinVar Variation:

50883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005918.1:p.Gly969Arg	CA351338 NM_001005918.3:c.2905G>A CA388026079 NM_001005918.3:c.2905G>C