Canonical Allele Identifier: PA2828231729
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 592120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354319.1:p.Ala17Val
CA378931933
NM_001367390.1:c.50C>T