Canonical Allele Identifier: PA2828231739
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719966
ClinVar RCV Id: RCV002305067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354319.1:p.Leu24Phe
CA378931775
NM_001367390.1:c.70C>T