Allele Registry

Canonical Allele Identifier: PA2826317900

Gene: ATP7B HGNC NCBI

ClinVar Allele:

18890

ClinVar RCV:

RCV000004055

RCV001091639

ClinVar Variation:

3851

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Ala763Val	CA252892 NM_001243182.2:c.2288C>T