Canonical Allele Identifier: PA2826317293
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 663268
ClinVar RCV Id: RCV000821118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Glu274Asp
CA388038675
NM_001243182.2:c.822A>T
CA388038678
NM_001243182.2:c.822A>C