Canonical Allele Identifier: PA2826581766
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 949981
ClinVar RCV Id: RCV001221584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Thr414Ala
CA374972121
NM_001278138.2:c.1240A>G