Canonical Allele Identifier: PA2825038248
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1979422
ClinVar RCV Id: RCV002766293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Tyr594Cys
CA250061586
NM_000053.4:c.1781A>G