Canonical Allele Identifier: PA2827326318
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Cys907Arg
CA260132
NM_001330578.2:c.2719T>C