Canonical Allele Identifier: PA2825279740
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Arg762Gln
CA252897
NM_001005918.3:c.2285G>A