Canonical Allele Identifier: PA645411402
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421884
ClinVar RCV Id: RCV000482531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Ala436Val
CA5786248
NM_021008.4:c.1307C>T