Canonical Allele Identifier: PA645400380
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 237022
ClinVar RCV Id: RCV000226902 RCV000664173 RCV000454429 RCV000488732 RCV001166478 RCV002399808 RCV002225526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Gly545Ser
CA5252712
NM_001114753.3:c.1633G>A