Canonical Allele Identifier: PA2827329449
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Arg868Lys
CA145676
NM_001330579.2:c.2603G>A