Canonical Allele Identifier: PA2826581643
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 414304
ClinVar RCV Id: RCV001084927 RCV003970317 RCV003640900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Val301Ile
CA5252756
NM_001278138.2:c.901G>A