Canonical Allele Identifier: PA2825044190
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 226041
ClinVar RCV Id: RCV000211433 RCV000859173 RCV002262803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Arg199His
CA5253073
NM_000118.3:c.596G>A