Canonical Allele Identifier: PA101238
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 161229
ClinVar RCV Id: RCV000148482 RCV000243657 RCV000230696 RCV000756073 RCV001079415 RCV002408654
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ser615Leu
CA211415
NM_001114753.3:c.1844C>T