Canonical Allele Identifier: PA916046690
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 126944
ClinVar RCV Id: RCV000114800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Gln1894Leu
CA151327
NM_001367624.2:c.5681A>T