Canonical Allele Identifier: PA091898
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 210482
ClinVar RCV Id: RCV000193403 RCV002254284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly591Asp
CA277133
NM_000053.4:c.1772G>A