Canonical Allele Identifier: PA2825280189
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 92389
ClinVar RCV Id: RCV000078053 RCV000490530 RCV002354273 RCV003333954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Val1090Ile
CA145689
NM_001005918.3:c.3268G>A