Canonical Allele Identifier: PA2826318109
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2083623
ClinVar RCV Id: RCV003002678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ala907Glu
CA388031755
NM_001243182.2:c.2720C>A