Canonical Allele Identifier: PA658659785
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458330
ClinVar RCV Id: RCV000559765 RCV000791352 RCV002367789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Glu41Lys
CA5253224
NM_001114753.3:c.121G>A