Allele Registry

Canonical Allele Identifier: PA2827325990

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000670079

RCV001509442

ClinVar Variation:

554444

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Thr772Ile	CA6988979 NM_001330578.2:c.2315C>T