Canonical Allele Identifier: PA2825044059
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 2043704
ClinVar RCV Id: RCV002913192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Gln166Arg
CA200314448
NM_000118.3:c.497A>G