Canonical Allele Identifier: PA2827329576
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 591446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Val913Met
CA388032133
NM_001330579.2:c.2737G>A