Canonical Allele Identifier: PA2827326952
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 188859
ClinVar RCV Id: RCV000169211 RCV000725176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Val1138Met
CA274052
NM_001330578.2:c.3412G>A