Canonical Allele Identifier: PA2825044579
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 570034
ClinVar RCV Id: RCV000690797 RCV001771949
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ala339Thr
CA5252899
NM_000118.3:c.1015G>A