Allele Registry

Canonical Allele Identifier: PA2827329006

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001527078

ClinVar Variation:

1172922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317508.1:p.Trp695Cys	CA388020479 NM_001330579.2:c.2085G>T CA388020480 NM_001330579.2:c.2085G>C