Canonical Allele Identifier: PA092051
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 430024
ClinVar RCV Id: RCV000494555 RCV000984147 RCV002527096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Tyr1331Ser
CA388020881
NM_000053.4:c.3992A>C