Canonical Allele Identifier: PA2827326778
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495415
ClinVar RCV Id: RCV000586771 RCV000666672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Arg1073His
CA6988682
NM_001330578.2:c.3218G>A