Canonical Allele Identifier: PA2825043932
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1299636
ClinVar RCV Id: RCV001730109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Leu99His
CA374986037
NM_000118.3:c.296T>A