Canonical Allele Identifier: PA2826581731
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407125
ClinVar RCV Id: RCV002261089 RCV003153610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Val386Ile
CA5252675
NM_001278138.2:c.1156G>A