Canonical Allele Identifier: PA2825279253
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1050375
ClinVar RCV Id: RCV001357726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.His344Tyr
CA388039424
NM_001005918.3:c.1030C>T