Canonical Allele Identifier: PA2827325002
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3072411
ClinVar RCV Id: RCV004013433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.His267Arg
CA388041311
NM_001330578.2:c.800A>G