Canonical Allele Identifier: PA2826317757
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 35706
ClinVar RCV Id: RCV000029355 RCV000078041 RCV002444440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Met658Val
CA171300
NM_001243182.2:c.1972A>G