Canonical Allele Identifier: PA645400288
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407122
ClinVar RCV Id: RCV000464848 RCV002481415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg197Trp
CA5253079
NM_001114753.3:c.589C>T