Canonical Allele Identifier: PA2826468626
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2963648
ClinVar RCV Id: RCV003825286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245283.1:p.Thr352Ala
CA399816069
NM_001258354.2:c.1054A>G