Canonical Allele Identifier: PA101061
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 661587
ClinVar RCV Id: RCV000819037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Cys363Ser
CA374980745
NM_001114753.3:c.1088G>C
CA374980747
NM_001114753.3:c.1087T>A