Canonical Allele Identifier: PA916009938
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 435060
ClinVar RCV Id: RCV000500817 RCV000633131 RCV001565138 RCV002367686 RCV004551628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Leu39Pro
CA374983528
NM_001278138.2:c.116T>C