Canonical Allele Identifier: PA2826581535
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 853374
ClinVar RCV Id: RCV001058168 RCV001819781 RCV002348428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Phe221Ser
CA374978484
NM_001278138.2:c.662T>C