Canonical Allele Identifier: PA2826317915
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 642900
ClinVar RCV Id: RCV000796453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr777Pro
CA388034454
NM_001243182.2:c.2329A>C