Canonical Allele Identifier: PA2827329226
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075609
ClinVar RCV Id: RCV004017127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile789Val
CA388034791
NM_001330579.2:c.2365A>G