Canonical Allele Identifier: PA916046562
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 379787
ClinVar RCV Id: RCV001720029 RCV002244876 RCV002392966 RCV003959886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Pro251Thr
CA8224622
NM_001367624.2:c.751C>A