Canonical Allele Identifier: PA2580227379
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768122
ClinVar RCV Id: RCV002387135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Gly3284Glu
CA397124898
NM_001367624.2:c.9851G>A