Canonical Allele Identifier: PA2826581538
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1751044
ClinVar RCV Id: RCV002358031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Leu223_Ser225delinsCys
CA2580079598
NM_001278138.2:c.668_673del