Canonical Allele Identifier: PA2827328267
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2077120
ClinVar RCV Id: RCV002972669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ser343Cys
CA388039441
NM_001330579.2:c.1028C>G