Canonical Allele Identifier: PA2826317286
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_001230111.1:p.Ile270Ser
CA250066843
NM_001243182.2:c.809T>G