Canonical Allele Identifier: PA2827329201
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2682332
ClinVar RCV Id: RCV003479705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala777Thr
CA388015392
NM_001330579.2:c.2329G>A