Canonical Allele Identifier: PA2825044482
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1475982
ClinVar RCV Id: RCV001977708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Lys291_Asp294del
CA2573143970
NM_000118.3:c.872_883del