Canonical Allele Identifier: PA2828231738
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2919495
ClinVar RCV Id: RCV003739383 RCV004374359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354319.1:p.Cys23Ser
CA378931787
NM_001367390.1:c.68G>C
CA378931796
NM_001367390.1:c.67T>A