Canonical Allele Identifier: PA2826318095
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2683626
ClinVar RCV Id: RCV003480446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Lys899Asn
CA388031895
NM_001243182.2:c.2697G>T
CA388031898
NM_001243182.2:c.2697G>C