Canonical Allele Identifier: PA2825280135
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3859
ClinVar RCV Id: RCV000004063 RCV000595271 RCV002354147 RCV003904803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asn1063Ser
CA252896
NM_001005918.3:c.3188A>G