Canonical Allele Identifier: PA916046678
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 320936
ClinVar RCV Id: RCV000368122 RCV000425667 RCV000432146 RCV002348060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Pro1696Leu
CA8225041
NM_001367624.2:c.5087C>T