Canonical Allele Identifier: PA916046630
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 126924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Lys1040Thr
CA151287
NM_001367624.2:c.3119A>C