Canonical Allele Identifier: PA2826468627
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637673
ClinVar RCV Id: RCV003404971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245283.1:p.Thr352Ser
CA399816064
NM_001258354.2:c.1055C>G
CA399816067
NM_001258354.2:c.1054A>T