Canonical Allele Identifier: PA2826317990
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 371483
ClinVar RCV Id: RCV000410917 RCV003480625
ClinVar Variation Id: 1409871
ClinVar RCV Id: RCV001916111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Trp828Cys
CA16041667
NM_001243182.2:c.2484G>T
CA388033509
NM_001243182.2:c.2484G>C