Canonical Allele Identifier: PA2826318341
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly1075Ser
CA274098
NM_001243182.2:c.3223G>A