Canonical Allele Identifier: PA916028294
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 558616
ClinVar RCV Id: RCV000674914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val946Ala
CA388030735
NM_001330578.2:c.2837T>C