Canonical Allele Identifier: PA891863935
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 592120
ClinVar RCV Id: RCV000723314 RCV002533074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Ala259Val
CA378931933
NM_021008.4:c.776C>T