Allele Registry

Canonical Allele Identifier: PA091981

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000004065

ClinVar Variation:

3861

HGVS (amino-acid)	Matching Registered Transcripts
NP_000044.2:p.Thr766Arg	CA252898 NM_000053.4:c.2297C>G