Allele Registry

Canonical Allele Identifier: PA2827324695

Gene: ATP7B HGNC NCBI

ClinVar Allele:

186912

ClinVar RCV:

RCV000169428

ClinVar Variation:

189037

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Gly85Val	CA274300 NM_001330578.2:c.254G>T