Canonical Allele Identifier: PA658660998
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 437396
ClinVar RCV Id: RCV000515532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Arg246Thr
CA378932296
NM_021008.4:c.737G>C