Canonical Allele Identifier: PA916028314
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly994Asp
CA388029839
NM_001330578.2:c.2981G>A