Canonical Allele Identifier: PA2826581633
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1204723
ClinVar RCV Id: RCV001571156 RCV002568459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Ser291Arg
CA374976591
NM_001278138.2:c.873C>G
CA374976592
NM_001278138.2:c.873C>A
CA374976606
NM_001278138.2:c.871A>C