Canonical Allele Identifier: PA2573200674
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1489862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Asn581Tyr
CA6989235
NM_001330579.2:c.1741A>T