Canonical Allele Identifier: PA916009957
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 439648
ClinVar RCV Id: RCV000508217 RCV001370738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Ala61Thr
CA5253001
NM_001278138.2:c.181G>A