Canonical Allele Identifier: PA2825279872
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 654991
ClinVar RCV Id: RCV000811070 RCV003155318 RCV003480854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asp840Tyr
CA388030195
NM_001005918.3:c.2518G>T