Canonical Allele Identifier: PA2827325726
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2060746
ClinVar RCV Id: RCV002947958 RCV002947957 RCV003395542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Leu641Val
CA250060805
NM_001330578.2:c.1921T>G