Canonical Allele Identifier: PA2827329966
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 977075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile1100Thr
CA250077094
NM_001330579.2:c.3299T>C