Canonical Allele Identifier: PA658659830
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458349
ClinVar RCV Id: RCV001764537 RCV002231269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Thr193Met
CA5253082
NM_001114753.3:c.578C>T