Canonical Allele Identifier: PA645411379
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 422488
ClinVar RCV Id: RCV000482280 RCV001171488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Glu239Gly
CA16619391
NM_021008.4:c.716A>G