Canonical Allele Identifier: PA2826318285
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 37122
ClinVar RCV Id: RCV000023582 RCV000727509 RCV002453275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ile1037Thr
CA259856
NM_001243182.2:c.3110T>C