Canonical Allele Identifier: PA645411383
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 422379
ClinVar RCV Id: RCV000487400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Arg254del
CA16619390
NM_021008.4:c.762_764del
CA378932092
NM_021008.4:c.760A>T