Canonical Allele Identifier: PA1139670651
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 881427
ClinVar RCV Id: RCV001110417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Val746Ile
CA6989081
NM_000053.4:c.2236G>A