Canonical Allele Identifier: PA2827326287
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Arg891Gln
CA252897
NM_001330578.2:c.2672G>A