Canonical Allele Identifier: PA091838
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3857
ClinVar RCV Id: RCV000004061 RCV001818123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Arg919Gly
CA252895
NM_000053.4:c.2755C>G