Canonical Allele Identifier: PA2826317348
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 633068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr322Ser
CA388036144
NM_001243182.2:c.965C>G
CA388036149
NM_001243182.2:c.964A>T