Canonical Allele Identifier: PA2825044735
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 652180
ClinVar RCV Id: RCV000807687 RCV003279087
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ala425Glu
CA374978152
NM_000118.3:c.1274C>A