Canonical Allele Identifier: PA916046798
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 419987
ClinVar RCV Id: RCV001704608 RCV003338606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Gly3284Arg
CA8225459
NM_001367624.2:c.9850G>A
CA397124895
NM_001367624.2:c.9850G>C