Allele Registry

Canonical Allele Identifier: PA2826581782

Gene: ENG HGNC NCBI

ClinVar RCV:

RCV000488791

ClinVar Variation:

426047

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265067.1:p.Arg436Leu	CA374970924 NM_001278138.2:c.1307G>T