Allele Registry

Canonical Allele Identifier: PA2827329595

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000145267

ClinVar Variation:

157943

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Gln920Pro	CA271174 NM_001330579.2:c.2759A>C