Allele Registry

Canonical Allele Identifier: PA091982

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000780926

RCV002223938

ClinVar Variation:

633064

HGVS (amino-acid)	Matching Registered Transcripts
NP_000044.2:p.Thr766Met	CA6989069 NM_000053.4:c.2297C>T