Canonical Allele Identifier: PA2827329511
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 556603
ClinVar RCV Id: RCV000672631 RCV003420191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Cys896Tyr
CA250082222
NM_001330579.2:c.2687G>A