Canonical Allele Identifier: PA2826318061
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188831
ClinVar RCV Id: RCV000169179 RCV000362786 RCV002433726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Pro881Leu
CA274013
NM_001243182.2:c.2642C>T