Canonical Allele Identifier: PA2826318023
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Arg858Gln
CA252897
NM_001243182.2:c.2573G>A