Canonical Allele Identifier: PA2827326588
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_001317507.1:p.Thr998Ala
CA388029811
NM_001330578.2:c.2992A>G