Canonical Allele Identifier: PA658660992
Gene: DEAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 437398
ClinVar RCV Id: RCV000515517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066288.2:p.Trp234Arg
CA378932679
NM_021008.4:c.700T>A
CA378932682
NM_021008.4:c.700T>C