Canonical Allele Identifier: PA2827044450
Gene: ZNF582 HGNC NCBI

Linked Data

ClinVar Variation Id: 102451
ClinVar RCV Id: RCV000088688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307300.2:p.Gly345Glu
CA229254
NM_001320371.4:c.1034G>A