Canonical Allele Identifier: PA145688
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35724
ClinVar RCV Id: RCV000029373 RCV000078052 RCV000755468 RCV002453269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.His1207Arg
CA145687
NM_000053.4:c.3620A>G