Canonical Allele Identifier: PA101251
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 665710
ClinVar RCV Id: RCV000824049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Val105Asp
CA374985916
NM_001114753.3:c.314T>A