Canonical Allele Identifier: PA2573200566
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1487801
ClinVar RCV Id: RCV002033640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Glu293Asp
CA388040710
NM_001330579.2:c.879G>T
CA388040714
NM_001330579.2:c.879G>C