Allele Registry

Canonical Allele Identifier: PA2827328962

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000004065

ClinVar Variation:

3861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Thr682Arg	CA252898 NM_001330579.2:c.2045C>G