Canonical Allele Identifier: PA2827325213
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1038648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ile381Ser
CA250066843
NM_001330578.2:c.1142T>G