Canonical Allele Identifier: PA2827325215
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 426499
ClinVar RCV Id: RCV000489206 RCV000613956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Ser382Cys
CA6989434
NM_001330578.2:c.1145C>G