Canonical Allele Identifier: PA2827328316
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3069703
ClinVar RCV Id: RCV004008247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly367Ser
CA250066886
NM_001330579.2:c.1099G>A