Canonical Allele Identifier: PA2826581537
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1750547
ClinVar RCV Id: RCV002355851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Val222Ala
CA374978466
NM_001278138.2:c.665T>C