Canonical Allele Identifier: PA2827325192
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1911929
ClinVar RCV Id: RCV002597321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr369Pro
CA6989442
NM_001330578.2:c.1105A>C