Canonical Allele Identifier: PA1139675574
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 834356
ClinVar RCV Id: RCV001035020 RCV001263065 RCV003480907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Gln166Pro
CA374984145
NM_001114753.3:c.497A>C