Canonical Allele Identifier: PA2827329571
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2093508
ClinVar RCV Id: RCV002996807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Met912Val
CA388032164
NM_001330579.2:c.2734A>G