Canonical Allele Identifier: PA2825280187
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 161207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asp1089Asn
CA272855
NM_001005918.3:c.3265G>A