Canonical Allele Identifier: PA2825805730
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2963648
ClinVar RCV Id: RCV003825286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136077.1:p.Thr327Ala
CA399816069
NM_001142605.2:c.979A>G