Canonical Allele Identifier: PA2828231722
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133294
ClinVar RCV Id: RCV000119807 RCV002514609 RCV003233107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354319.1:p.Arg12Ser
CA156401
NM_001367390.1:c.36A>C
CA378932074
NM_001367390.1:c.36A>T