Canonical Allele Identifier: PA916028270
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 420002
ClinVar RCV Id: RCV000631248 RCV001263514 RCV000587060 RCV002525825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Leu641Ser
CA6989172
NM_001330578.2:c.1922T>C