Canonical Allele Identifier: PA658802318
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 526655
ClinVar RCV Id: RCV000631234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000044.2:p.Asp642Tyr
CA388027513
NM_000053.4:c.1924G>T