Canonical Allele Identifier: PA2825038622
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1163547
ClinVar RCV Id: RCV001508715 RCV001882558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1006Asp
CA388031972
NM_000053.4:c.3017G>A