Canonical Allele Identifier: PA2827326751
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1134697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala1061Gly
CA6988690
NM_001330578.2:c.3182C>G