Canonical Allele Identifier: PA2827325639
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1722021
ClinVar RCV Id: RCV002295094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Tyr594Ser
CA388030593
NM_001330578.2:c.1781A>C