Canonical Allele Identifier: PA916046704
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 320955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Arg2157Lys
CA8225159
NM_001367624.2:c.6470G>A