Canonical Allele Identifier: PA2825279686
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1498975
ClinVar RCV Id: RCV002035678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly719Ser
CA388034612
NM_001005918.3:c.2155G>A