Canonical Allele Identifier: PA2825038493
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3074623
ClinVar RCV Id: RCV004014157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Pro863Arg
CA388015300
NM_000053.4:c.2588C>G