Canonical Allele Identifier: PA2827327292
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157955
ClinVar RCV Id: RCV000145280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly1263Ser
CA271177
NM_001330578.2:c.3787G>A