Canonical Allele Identifier: PA916046378
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 437396
ClinVar RCV Id: RCV000515532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354319.1:p.Arg4Thr
CA378932296
NM_001367390.1:c.11G>C