Canonical Allele Identifier: PA2825044731
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 2913043
ClinVar RCV Id: RCV003760528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Glu424Val
CA374978220
NM_000118.3:c.1271A>T