Canonical Allele Identifier: PA2827326095
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_001317507.1:p.Asn814Ser
CA6988939
NM_001330578.2:c.2441A>G