Canonical Allele Identifier: PA2741908847
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637673
ClinVar RCV Id: RCV003404971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004238.3:p.Thr362Ser
CA399816064
NM_004247.4:c.1085C>G
CA399816067
NM_004247.4:c.1084A>T