Allele Registry

Canonical Allele Identifier: PA2825279679

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001322608

ClinVar Variation:

1022669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005918.1:p.Ala712Glu	CA388034776 NM_001005918.3:c.2135C>A