Canonical Allele Identifier: PA2826581321
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_001265067.1:p.Thr11Met
CA5253082
NM_001278138.2:c.32C>T