Canonical Allele Identifier: PA2825280052
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35724
ClinVar RCV Id: RCV000029373 RCV000078052 RCV000755468 RCV002453269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.His1000Arg
CA145687
NM_001005918.3:c.2999A>G