Allele Registry

Canonical Allele Identifier: PA2825044297

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV002234424

ClinVar Variation:

528069

HGVS (amino-acid)	Matching Registered Transcripts
NP_000109.1:p.Pro225Ala	CA374983508 NM_000118.3:c.673C>G