Canonical Allele Identifier: PA2580227395
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 2083237
ClinVar RCV Id: RCV003002378 RCV004068395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Pro3327Leu
CA286386051
NM_001367624.2:c.9980C>T