Canonical Allele Identifier: PA2826318010
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 928975
ClinVar RCV Id: RCV001193694 RCV001833746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Tyr842Ser
CA6988896
NM_001243182.2:c.2525A>C