Canonical Allele Identifier: PA2827326788
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075591
ClinVar RCV Id: RCV004017109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Trp1075Gly
CA388026586
NM_001330578.2:c.3223T>G