Canonical Allele Identifier: PA645400382
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407135
ClinVar RCV Id: RCV000458266 RCV003151063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Cys549Tyr
CA500023
NM_001114753.3:c.1646G>A