Allele Registry

Canonical Allele Identifier: PA2499227092

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001322608

ClinVar Variation:

1022669

HGVS (amino-acid)	Matching Registered Transcripts
NP_000044.2:p.Ala874Glu	CA388034776 NM_000053.4:c.2621C>A