Canonical Allele Identifier: PA2827326064
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1498975
ClinVar RCV Id: RCV002035678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly803Ser
CA388034612
NM_001330578.2:c.2407G>A