Canonical Allele Identifier: PA2826318302
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2154616
ClinVar RCV Id: RCV003069373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly1047Arg
CA6988676
NM_001243182.2:c.3139G>C