Canonical Allele Identifier: PA2825805728
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637673
ClinVar RCV Id: RCV003404971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136077.1:p.Thr327Ser
CA399816064
NM_001142605.2:c.980C>G
CA399816067
NM_001142605.2:c.979A>T