Canonical Allele Identifier: PA2825279926
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3073800
ClinVar RCV Id: RCV004016806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Glu879Asp
CA388028923
NM_001005918.3:c.2637G>T
CA388028926
NM_001005918.3:c.2637G>C