Canonical Allele Identifier: PA2826468294
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637673
ClinVar RCV Id: RCV003404971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245282.1:p.Thr362Ser
CA399816064
NM_001258353.2:c.1085C>G
CA399816067
NM_001258353.2:c.1084A>T