Canonical Allele Identifier: PA2573179428
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1358073
ClinVar RCV Id: RCV001878539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ser16Arg
CA5253262
NM_001114753.3:c.48C>G
CA374989567
NM_001114753.3:c.48C>A
CA374989576
NM_001114753.3:c.46A>C