Canonical Allele Identifier: PA916046795
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 808135
ClinVar RCV Id: RCV000996373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Ser3244Pro
CA397124592
NM_001367624.2:c.9730T>C