Allele Registry

Canonical Allele Identifier: PA2827329594

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV004013829

ClinVar Variation:

3072807

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Gln920Arg	CA388032008 NM_001330579.2:c.2759A>G