Canonical Allele Identifier: PA2826581650
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_001265067.1:p.Leu308Ser
CA5252752
NM_001278138.2:c.923T>C