Canonical Allele Identifier: PA2826581792
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1782359
ClinVar RCV Id: RCV002408314 RCV003418519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Ser453Leu
CA5252585
NM_001278138.2:c.1358C>T