Canonical Allele Identifier: PA091973
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 556435
ClinVar RCV Id: RCV000672441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr1029Ile
CA388030555
NM_000053.4:c.3086C>T