Canonical Allele Identifier: PA2825038849
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3072663
ClinVar RCV Id: RCV004013685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Ala1205Thr
CA388024279
NM_000053.4:c.3613G>A