Canonical Allele Identifier: PA2825044921
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407135
ClinVar RCV Id: RCV000458266 RCV003151063
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Cys549Tyr
CA500023
NM_000118.3:c.1646G>A