Canonical Allele Identifier: PA101261
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407121
ClinVar RCV Id: RCV000460714 RCV001753879 RCV002365627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Val238Glu
CA16612408
NM_001114753.3:c.713T>A