Canonical Allele Identifier: PA2825279907
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly865Asp
CA388029839
NM_001005918.3:c.2594G>A