Canonical Allele Identifier: PA645411394
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423408
ClinVar RCV Id: RCV000485882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Ile256Asn
CA16619389
NM_021008.4:c.767T>A