Canonical Allele Identifier: PA2826468429
Gene: EFTUD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374152
ClinVar RCV Id: RCV000415160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245282.1:p.Asn683Tyr
CA16043528
NM_001258353.2:c.2047A>T