Canonical Allele Identifier: PA2827326895
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1513874
ClinVar RCV Id: RCV002018502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ala1117Val
CA388024554
NM_001330578.2:c.3350C>T