Canonical Allele Identifier: PA2827325148
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1771226
ClinVar RCV Id: RCV002381104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.His344Arg
CA388039418
NM_001330578.2:c.1031A>G