Canonical Allele Identifier: PA2827330100
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile1146Val
CA6988609
NM_001330579.2:c.3436A>G