Canonical Allele Identifier: PA2825280096
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 456557
ClinVar RCV Id: RCV000541103 RCV001507826 RCV002350175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Val1032Gly
CA6988580
NM_001005918.3:c.3095T>G