Canonical Allele Identifier: PA101206
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458338
ClinVar RCV Id: RCV000539445 RCV002395314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Leu490Ser
CA5252752
NM_001114753.3:c.1469T>C