Canonical Allele Identifier: PA2825279948
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 370820
ClinVar RCV Id: RCV000410034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly892Ser
CA6988744
NM_001005918.3:c.2674G>A