Canonical Allele Identifier: PA2499238134
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1015736
ClinVar RCV Id: RCV001314641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg399Ser
CA374978541
NM_001114753.3:c.1197G>T
CA374978543
NM_001114753.3:c.1197G>C