Canonical Allele Identifier: PA2827328366
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1923419
ClinVar RCV Id: RCV002604629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ile390Met
CA388038585
NM_001330579.2:c.1170A>G