Canonical Allele Identifier: PA916046800
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 392331
ClinVar RCV Id: RCV002244926 RCV001696836 RCV002379387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Arg3345His
CA8225471
NM_001367624.2:c.10034G>A