Allele Registry

Canonical Allele Identifier: PA2827329947

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001852911

ClinVar Variation:

50883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Gly1092Arg	CA351338 NM_001330579.2:c.3274G>A CA388026079 NM_001330579.2:c.3274G>C