Canonical Allele Identifier: PA2825038730
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2026537
ClinVar RCV Id: RCV002858414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gln1095Arg
CA388028724
NM_000053.4:c.3284A>G