Canonical Allele Identifier: PA913191866
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 617913
ClinVar RCV Id: RCV000755719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Gly591Ser
CA388030768
NM_000053.4:c.1771G>A