Canonical Allele Identifier: PA2826318213
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073800
ClinVar RCV Id: RCV004016806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Glu975Asp
CA388028923
NM_001243182.2:c.2925G>T
CA388028926
NM_001243182.2:c.2925G>C