Canonical Allele Identifier: PA2825038801
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2154616
ClinVar RCV Id: RCV003069373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly1158Arg
CA6988676
NM_000053.4:c.3472G>C