Canonical Allele Identifier: PA2825579069
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1744257
ClinVar RCV Id: RCV002342674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Pro165Ala
CA374984153
NM_001114753.3:c.493C>G