Canonical Allele Identifier: PA107485
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133294
ClinVar RCV Id: RCV000119807 RCV002514609 RCV003233107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Arg254Ser
CA156401
NM_021008.4:c.762A>C
CA378932074
NM_021008.4:c.762A>T