Canonical Allele Identifier: PA2827329282
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2139980
ClinVar RCV Id: RCV003066731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Asn808Ser
CA6988939
NM_001330579.2:c.2423A>G