Canonical Allele Identifier: PA2826318512
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 189149
ClinVar RCV Id: RCV000169572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Leu1188Phe
CA274423
NM_001243182.2:c.3562C>T