Canonical Allele Identifier: PA2825038521
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1930912
ClinVar RCV Id: RCV002631301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr894Ala
CA388034344
NM_000053.4:c.2680A>G