Canonical Allele Identifier: PA2825038691
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 663298
ClinVar RCV Id: RCV000821152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Thr1062Ile
CA6988784
NM_000053.4:c.3185C>T