Allele Registry

Canonical Allele Identifier: PA2827326952

Gene: ATP7B HGNC NCBI

ClinVar Allele:

186878

ClinVar RCV:

RCV000169211

RCV000725176

ClinVar Variation:

188859

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Val1138Met	CA274052 NM_001330578.2:c.3412G>A