Canonical Allele Identifier: PA2827326212
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr857Met
CA273878
NM_001330578.2:c.2570C>T