Canonical Allele Identifier: PA916028351
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 312397
ClinVar RCV Id: RCV000354484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Arg226Trp
CA6989517
NM_001330579.2:c.676C>T