Allele Registry

Canonical Allele Identifier: PA2827327197

Gene: ATP7B HGNC NCBI

ClinVar Allele:

186875

ClinVar RCV:

RCV000169572

ClinVar Variation:

189149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Leu1221Phe	CA274423 NM_001330578.2:c.3661C>T