Canonical Allele Identifier: PA2827326883
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 591311
ClinVar RCV Id: RCV000722489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Met1113Val
CA388024703
NM_001330578.2:c.3337A>G