Canonical Allele Identifier: PA2826318034
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35710
ClinVar RCV Id: RCV000029359 RCV000790662 RCV002433469 RCV003924861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr866Met
CA220308
NM_001243182.2:c.2597C>T