Canonical Allele Identifier: PA2825279658
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1501800
ClinVar RCV Id: RCV002019924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr696Ala
CA388015660
NM_001005918.3:c.2086A>G