Canonical Allele Identifier: PA2827328761
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2198694
ClinVar RCV Id: RCV002633808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Phe608Ser
CA250061564
NM_001330579.2:c.1823T>C