Canonical Allele Identifier: PA2826318338
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 977075
ClinVar RCV Id: RCV001254597 RCV001751521 RCV002451623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ile1073Thr
CA250077094
NM_001243182.2:c.3218T>C