Canonical Allele Identifier: PA145662
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 92381
ClinVar RCV Id: RCV000078033 RCV000640913 RCV002277140 RCV002313747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000043.4:p.Tyr608Cys
CA145661
NM_000052.7:c.1823A>G