Canonical Allele Identifier: PA2825279767
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 374060
ClinVar RCV Id: RCV000415306 RCV001198322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly781Glu
CA16043475
NM_001005918.3:c.2342G>A