Canonical Allele Identifier: PA2827326298
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 862055
ClinVar RCV Id: RCV001068702 RCV002254330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ser897Tyr
CA6988860
NM_001330578.2:c.2690C>A