Canonical Allele Identifier: PA2827325322
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495399
ClinVar RCV Id: RCV000589895 RCV001459906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Cys431Arg
CA6989382
NM_001330578.2:c.1291T>C