Allele Registry

Canonical Allele Identifier: PA2825279801

Gene: ATP7B HGNC NCBI

ClinVar Allele:

167790

ClinVar RCV:

RCV000145267

ClinVar Variation:

157943

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005918.1:p.Gln797Pro	CA271174 NM_001005918.3:c.2390A>C