Canonical Allele Identifier: PA2827326013
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2682332
ClinVar RCV Id: RCV003479705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala783Thr
CA388015392
NM_001330578.2:c.2347G>A