Canonical Allele Identifier: PA2827329964
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 374482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile1100Val
CA16043757
NM_001330579.2:c.3298A>G