Allele Registry

Canonical Allele Identifier: PA2827327089

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV002248978

ClinVar Variation:

1685251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Asn1192Ile	CA6988565 NM_001330578.2:c.3575A>T