Canonical Allele Identifier: PA2828231720
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_001354319.1:p.Arg12del
CA16619390
NM_001367390.1:c.36_38del
CA378932092
NM_001367390.1:c.34A>T