Canonical Allele Identifier: PA2826581758
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 237024
ClinVar RCV Id: RCV000233031 RCV000414391 RCV001169423 RCV002408948 RCV003221872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Val406Ile
CA5252632
NM_001278138.2:c.1216G>A