Canonical Allele Identifier: PA913199099
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157928
ClinVar RCV Id: RCV000145251 RCV000416017 RCV002514798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Asn41Ser
CA271166
NM_001005918.3:c.122A>G