Canonical Allele Identifier: PA645400218
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 374952
ClinVar RCV Id: RCV000415646 RCV000488039 RCV001034662 RCV001821144 RCV002418240 RCV003950330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg3Cys
CA5253268
NM_001114753.3:c.7C>T