Canonical Allele Identifier: PA2826317916
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1516399
ClinVar RCV Id: RCV002023924 RCV002509746 RCV002548851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr777Ser
CA388034452
NM_001243182.2:c.2330C>G
CA388034459
NM_001243182.2:c.2329A>T