Canonical Allele Identifier: PA2827329910
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 811257
ClinVar RCV Id: RCV001001003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly1074Val
CA6988675
NM_001330579.2:c.3221G>T