Canonical Allele Identifier: PA2828231735
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098659
ClinVar RCV Id: RCV003031057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354319.1:p.Leu21Ser
CA378931835
NM_001367390.1:c.62T>C