Canonical Allele Identifier: PA2827329653
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 526658
ClinVar RCV Id: RCV000631238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr949Ala
CA388030499
NM_001330579.2:c.2845A>G