Canonical Allele Identifier: PA2827330000
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 555617
ClinVar RCV Id: RCV000671472 RCV001805793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Ala1113Thr
CA6988627
NM_001330579.2:c.3337G>A