Canonical Allele Identifier: PA2580227363
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767681
ClinVar RCV Id: RCV002385385 RCV003718576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Gly3246Ser
CA8225450
NM_001367624.2:c.9736G>A