Allele Registry

Canonical Allele Identifier: PA2827326006

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000430661

RCV000667536

ClinVar Variation:

377538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Ile779Thr	CA16606473 NM_001330578.2:c.2336T>C