Canonical Allele Identifier: PA2827326776
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 623152
ClinVar RCV Id: RCV000761257 RCV002286787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly1071Ala
CA388026664
NM_001330578.2:c.3212G>C