Canonical Allele Identifier: PA2825279915
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3071932
ClinVar RCV Id: RCV004011962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr869Ala
CA388029811
NM_001005918.3:c.2605A>G