Canonical Allele Identifier: PA2741873160
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683382
ClinVar RCV Id: RCV003480202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Ser3301Ile
CA397125062
NM_001367624.2:c.9902G>T