Canonical Allele Identifier: PA220310
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.His958Gln
CA220309
NM_001243182.2:c.2874C>A
CA388029876
NM_001243182.2:c.2874C>G