Canonical Allele Identifier: PA2826318414
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 456557
ClinVar RCV Id: RCV000541103 RCV001507826 RCV002350175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Val1128Gly
CA6988580
NM_001243182.2:c.3383T>G