Canonical Allele Identifier: PA2827326269
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2420390
ClinVar RCV Id: RCV003118915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Asn880Ser
CA388032571
NM_001330578.2:c.2639A>G