Canonical Allele Identifier: PA2826581432
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1970199
ClinVar RCV Id: RCV002760341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Cys148Phe
CA374981865
NM_001278138.2:c.443G>T