Canonical Allele Identifier: PA2828245003
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232886
ClinVar RCV Id: RCV004523518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Ala3245Thr
CA397124598
NM_001367624.2:c.9733G>A