Canonical Allele Identifier: PA2825279295
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1038648
ClinVar RCV Id: RCV001341983 RCV002456483 RCV003331123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Ile381Ser
CA250066843
NM_001005918.3:c.1142T>G