Canonical Allele Identifier: PA2499238152
Gene: ENG HGNC NCBI
ClinVar RCV:
RCV001312394
ClinVar Variation:
1013753
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Cys582Gly
CA374972338
NM_001114753.3:c.1744T>G