Allele Registry

Canonical Allele Identifier: PA2826317753

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000410970

ClinVar Variation:

370887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Pro657Leu	CA16041671 NM_001243182.2:c.1970C>T