Canonical Allele Identifier: PA916046794
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 321006
ClinVar RCV Id: RCV000308943 RCV001837823 RCV002379202 RCV003957655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.His3226Asn
CA10638622
NM_001367624.2:c.9676C>A