Canonical Allele Identifier: PA2826317667
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495405
ClinVar RCV Id: RCV000586389 RCV003326468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly600Arg
CA388023470
NM_001243182.2:c.1798G>C
CA388023479
NM_001243182.2:c.1798G>A