Canonical Allele Identifier: PA2825279892
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 370081
ClinVar RCV Id: RCV000411652 RCV001091637 RCV002323574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Glu857Ala
CA6988781
NM_001005918.3:c.2570A>C