Canonical Allele Identifier: PA107475
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133293
ClinVar RCV Id: RCV000119806 RCV001310582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Arg224Trp
CA156399
NM_021008.4:c.670C>T