Canonical Allele Identifier: PA2825579211
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 2182776
ClinVar RCV Id: RCV002611022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Lys285Arg
CA374982694
NM_001114753.3:c.854A>G