Canonical Allele Identifier: PA2826317659
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3865
ClinVar RCV Id: RCV000004069 RCV000507833 RCV000597397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Leu597Pro
CA252902
NM_001243182.2:c.1790T>C