Canonical Allele Identifier: PA2825280135
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asn1063Ser
CA252896
NM_001005918.3:c.3188A>G