Canonical Allele Identifier: PA645411375
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391596
ClinVar RCV Id: RCV000443903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Trp234Gly
CA16606380
NM_021008.4:c.700T>G