ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA112888
Gene: EFTUD2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000023353
RCV001794462
ClinVar Variation:
30400
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245282.1:p.Arg262Trp
CA259795
NM_001258353.2:c.784C>T