Canonical Allele Identifier: PA2573193573
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1432409
ClinVar RCV Id: RCV001941245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Asp82_Asn84del
CA2573143975
NM_001278138.2:c.244_252del