Canonical Allele Identifier: PA658803114
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528060
ClinVar RCV Id: RCV000633140
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ser615Trp
CA5252623
NM_001114753.3:c.1844C>G