Canonical Allele Identifier: PA2826317284
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2127867
ClinVar RCV Id: RCV003036059 RCV003348983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Met269Leu
CA388038787
NM_001243182.2:c.805A>T
CA388038792
NM_001243182.2:c.805A>C