Canonical Allele Identifier: PA2827329955
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2794286
ClinVar RCV Id: RCV003609543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr1094Pro
CA388026029
NM_001330579.2:c.3280A>C