Canonical Allele Identifier: PA2826318328
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 959197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr1067Ala
CA388026028
NM_001243182.2:c.3199A>G