Canonical Allele Identifier: PA2825579240
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1970199
ClinVar RCV Id: RCV002760341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Cys330Phe
CA374981865
NM_001114753.3:c.989G>T