Canonical Allele Identifier: PA2826581687
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 213212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Arg347His
CA321073
NM_001278138.2:c.1040G>A