Canonical Allele Identifier: PA2580227358
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767577
ClinVar RCV Id: RCV003103598 RCV002385327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Thr3232Met
CA286385653
NM_001367624.2:c.9695C>T